Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families

Authors


Dr Morteza Hashemzadeh Chaleshtori, PhD
Cellular and Molecular Research Center
Shahrekord University of Medical Sciences
Shahrekord
Iran
Tel: +98 381 3346692
Fax: +98 381 3330709
e-mail: mchalesh@yahoo.com

No abstract is available for this article.

Ancillary